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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086268Generated: November 3, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 131716919, compound

https://huagongshe.com/reaction/1086268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(1,2,3,4-Tetrahydronaphthalen-2-yl)acetic acidHCID 10012739—
ReactantEthyl (4R)-4-thiazolidinecarboxylateHCID 13011878—
SolventDichloromethaneHCID 6344—
ProductHCID 131716919HCID 13171691968.5%

Reaction Steps

To a mixture of 2.85 g of 1,2,3,4-tetrahydronaphthalen-2-ylacetic acid and 13.45 g of WSC.HCl was added 45 ml of methylene chloride under ice-cooling. The mixture was stirred for 5 minutes at room temperature. To this was added a solution of 2.4 g of L-thioproline ethyl ester in 7 ml of methylene chloride at room temperature, and the mixture was stirred for a further 18 hours at the same temperature. The reaction mixture was washed with water, diluted hydrochloric acid, and saturated sodium hydrogen carbonate in this order. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue thus obtained was purified by silica gel column chromatography to produce 3.4 g of 3-(1,2,3,4-tetrahydronaphthalen-2-ylacetyl)-L-thioproline ethyl ester as a colorless oil (yield: 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028604
Source datasetuspto-grants-1991_07
ORD IDord-a66faf0c329b428184a153c0d46eec24
Source noteuspto-grants-1991_07